rs727504356

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs727504356(C;C)

Make rs727504356(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23424846

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs727504356
dbSNP (classic)	rs727504356
ClinGen	rs727504356
ebi	rs727504356
HLI	rs727504356
Exac	rs727504356
Gnomad	rs727504356
Varsome	rs727504356
LitVar	rs727504356
Map	rs727504356
PheGenI	rs727504356
Biobank	rs727504356
1000 genomes	rs727504356
hgdp	rs727504356
ensembl	rs727504356
geneview	rs727504356
scholar	rs727504356
google	rs727504356
pharmgkb	rs727504356
gwascentral	rs727504356
openSNP	rs727504356
23andMe	rs727504356
SNPshot	rs727504356
SNPdbe	rs727504356
MSV3d	rs727504356
GWAS Ctlg	rs727504356

Max Magnitude

0

ClinVar
Risk	rs727504356(C;C)
Alt	rs727504356(C;C)
Reference	Rs727504356(G;G)
Significance	Pathogenic
Disease	not specified Hypertrophic cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	not specified Hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23894055C>G
CLNSRC
CLNACC	RCV000154484.3, RCV000475271.1,